Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE

被引:3
作者
Zhang, Xin [1 ]
Liu, Lirong [1 ,2 ]
Ma, Xiaolei [1 ]
Hu, Wei [3 ]
Xu, Xue [1 ]
Huang, Saisai [1 ]
Hua, Bingzhu [1 ]
Wang, Hong [1 ]
Chen, Zhiyong [1 ]
Sun, Lingyun [1 ]
机构
[1] Nanjing Univ, Affiliated Drum Tower Hosp, Dept Rheumatol & Immunol, Med Sch, Nanjing, Peoples R China
[2] First Hosp Changshu, Dept Rheumatol & Immunol, Changshu, Jiangsu, Peoples R China
[3] Nanjing Univ, Med Sch, Affiliated Drum Tower Hosp, Dept Clin Lab, Nanjing, Peoples R China
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; MYOCARDIAL-INFARCTION; METABOLIC SYNDROME; RISK; THERAPY; RATIO; DYSLIPOPROTEINEMIA; ASSOCIATION; PREVALENCE; WOMEN;
D O I
10.1371/journal.pone.0231622
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objectives Nonthyroidal illness syndrome (NTIS), also known as low triiodothyronine (T3) syndrome, frequently affects patients with systemic lupus erythematosus (SLE) and may affect lipid metabolism. Dyslipidemia is highly prevalent and associated with the long-term prognosis of SLE. The aim of the present study was to explore the clinical significance of NTIS on disease activity and dyslipidemia in patients with SLE. Methods Clinical and laboratory data were collected retrospectively from 223 patients with SLE. The correlation between free triiodothyronine (FT3), SLE disease activity, and lipid profiles were estimated. The correlation coefficient (r) was calculated using a Pearson's regression model. Univariate and multivariate logistic regression analyses were performed to identify the risk factors for dyslipidemia in SLE. Results Serum FT3 levels were negatively correlated with the levels of 24 h urine protein (UP), blood urea nitrogen (BUN), creatinine (Cr) and SLE disease activity index (SLEDAI) (all p < 0.001) in NTIS patients but not in euthyroid patients. ApoB/ApoA1 was significantly correlated with SLEDAI (p < 0.01) in NTIS patients and CRP (p < 0.001) and ESR (p < 0.01) in euthyroid patients. A multivariate analysis revealed that only FT3 exhibited an independent negative association with dyslipidemia (P = 0.01; OR = 0.48; 95% CI 0.27-0.85). Conclusion NTIS frequently occurs in patients with SLE. Low FT3 is associated with disease activity in SLE patients complicated with NTIS. Low FT3 is an independent risk factor for dyslipidemia in patients with SLE.
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